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Sample GSM8382773 Query DataSets for GSM8382773
Status Public on Jul 09, 2024
Title Patient 3 at (T0)
Sample type RNA
 
Source name Peripheral Blood Mononuclear Cells (PBMCs) before surgery
Organism Homo sapiens
Characteristics gender: Male
age: 46
type of surgery: Biliopacreatic Diversion without duodenal switch
phenotype: Responder
tissue: PBMCs
Extracted molecule total RNA
Extraction protocol The total RNA was extracted from PBMCs using the SV Total RNA Isolation Kit from Promega following the manufacturer's instructions.
Label biotin
Label protocol 500 ng of total RNA were used to synthesis cDNA and preparing biotinylated cRNA according to the Affymetrix protocol
 
Hybridization protocol 11 µg of labeled and fragmented cRNA were hybridized for 16 hours at 54 C on Affymetrix Human Genome U133 Plus 2.0 Array. After that, washing and staining of the GeneChips were performed using the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Description Gene expression data from obese patient before the bariatric surgery
Data processing We processed the raw CEL files using freely available updated chip definition files (CDF) for HG-U 133 Plus 2.0 arrays based on Entrez genes, which remaps every probe in the array, re-aligning to the sequences of the latest genome assembly. Specifically, we used three libraries of version 22, namely HG-U 133 Plus 2.0 Entrez gcdf, HG-U 133 Plus 2.0 Entrez gprobe, and HG-U 133 Plus 2.0 Entrez gdb (2) from http://mbni.org/customcdf/22.0.0. We imported and converted the probe intensity data from the CEL files along with the above-mentioned CDF file into the probe level ‘AffyBatch’ object by ReadAffy function of the Affy R package in Bioconductor (3). We imported the phenotypic data using the pData function into the AffyBatch object. Finally, we used (4)the RMA function on this object for background correction, normalization of the multiple array data using the Robust Multiarray Average (RMA) method, and expression calculation for the entire probes available in the CDF file. This step produces an object containing probe level expression matrix. We populated the probe level feature data into this ‘Expression Set’ object using annotateEset function of the R package ‘affycoretools’ and chipDB object (hgu133plus2hsrefseq.db) from the brain array project. Then, we used the ‘exprs’ function in the Affy package to extract the expression matrix of the genes / probes for further downstream analyzes.
 
Submission date Jul 08, 2024
Last update date Jul 09, 2024
Contact name Abderrezak Bouchama
E-mail(s) rezakbouchama@gmail.com
Organization name KAIMRC
Department Experimental Medicine
Street address Ahmad Ibn Hanbal Street, Ar Rimayah
City Riyadh
ZIP/Postal code 11481
Country Saudi Arabia
 
Platform ID GPL34684
Series (1)
GSE271700 Transcriptome Changes and Metabolic Outcomes After Bariatric Surgery in Adults With Obesity and Type 2 Diabetes

Data table header descriptions
ID_REF
VALUE normalized probe signal intensity

Data table
ID_REF VALUE
1_at 6.0501
503538_at 4.2947
29974_at 3.565
2_at 5.0291
144571_at 6.9278
144568_at 3.4332
53947_at 4.3948
51146_at 4.4015
100506677_at 4.4239
8086_at 5.9321
65985_at 6.6289
729522_at 2.9009
13_at 4.5321
344752_at 2.5584
201651_at 3.0809
51166_at 3.9733
195827_at 7.7423
79719_at 5.9645
22848_at 5.5179
28971_at 5.5324

Total number of rows: 20158

Table truncated, full table size 318 Kbytes.




Supplementary file Size Download File type/resource
GSM8382773_T0_DM05_81_R.CEL.gz 4.5 Mb (ftp)(http) CEL

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